Jansen干骺端软骨发育不良:颅面表现分析。

IF 3.4 Q2 ENDOCRINOLOGY & METABOLISM
JBMR Plus Pub Date : 2024-11-26 eCollection Date: 2025-02-01 DOI:10.1093/jbmrpl/ziae156
Fiona Obiezu, Konstantinia Almpani, Hung Jeffrey Kim, Christopher Zalewski, Emily Chu, Golnar Jahanmir, Kelly L Roszko, Alison Boyce, Faraz Farhadi, Lee S Weinstein, Rachel I Gafni, Carlos R Ferreira, Harald Jüppner, Michael T Collins, Janice S Lee, Smita Jha
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引用次数: 0

摘要

Jansen干骺端软骨发育不良(JMC)是一种由甲状旁腺激素1型受体(PTH1R)组成性激活引起的罕见疾病。我们试图描述该疾病患者的颅面表型。6例遗传确诊的JMC患者接受了全面的颅面表型分析,显示出明显的面部外观,这促使头侧测量分析显示出下颌后颌畸形的模式。口腔检查:上颚扁平浅,出牙延迟,上颌牙阻生。研究的5名患者中有4名出现亚临床和/或轻度听力损失。最常见的病因是传导性的,可能是由于上腔过度拥挤,阻碍了听小骨的正常振动。6例患者中5例鼻窦闭塞。颅面骨的计算机断层扫描(CT)评估显示双侧对称的扩张性病变,主要累及神经嵴细胞(NCC)来源的骨骼。与年龄匹配的对照组相比,6例患者中有5例出现双侧面神经管狭窄,特别是迷路段;1例患者表现为进行性面神经麻痹。6例患者中有5例存在矢状缝缝性颅缝闭塞,其中1例有婴儿期全缝闭塞颅脑重建术史。所有患者均表现出明显程度的上气道狭窄,以及更多的前舌骨移位。两名患者被诊断为阻塞性睡眠呼吸暂停。18F-NaF正电子发射断层扫描(PET)-CT显示,所有患者的颅底和颌骨摄取增加。总之,对JMC患者颅面表型的首次详细系统评估表明,一种独特而明显的表型主要影响nc源性颅骨,表明PTH1R信号在其发育中起关键作用。这些影响可导致显著的疾病相关发病率,包括听力损失、神经压迫、颅缝紧闭、牙骨错颌和气道损伤;所有这些都需要密切监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Jansen metaphyseal chondrodysplasia: analysis of craniofacial manifestations.

Jansen metaphyseal chondrodysplasia (JMC) is an ultra-rare disorder caused by constitutive activation of parathyroid hormone type 1 receptor (PTH1R). We sought to characterize the craniofacial phenotype of patients with the disease. Six patients with genetically confirmed JMC underwent comprehensive craniofacial phenotyping revealing a distinct facial appearance that prompted a cephalometric analysis demonstrating a pattern of mandibular retrognathia. Oral examination was notable for flat and shallow palate, delayed eruption pattern, and impacted maxillary teeth. Subclinical and/or mild hearing loss was noted in 4 of 5 patients studied. The most common etiology was conductive, likely due to overcrowding of epitympanum which impedes the normal vibration of ossicles to sound. Paranasal sinus obliteration was noted in 5 of 6 patients. Computed tomography (CT) scan evaluation of craniofacial bones revealed bilaterally symmetric expansile lesions with predominant involvement of neural crest cell (NCC)-derived bones. Bilateral narrowing of facial nerve canals, particularly at the labyrinthine segment, was seen in 5 of 6 patients when compared to age-matched controls; 1 patient presented with progressive facial nerve palsy. Sagittal suture craniosynostosis was present in 5 of 6 patients-one of whom had a history of cranial reconstruction for pansynostosis in infancy. All patients demonstrated a significant degree of upper airway stenosis, as well as a more anterior hyoid bone displacement. Two patients had a diagnosis of obstructive sleep apnea. 18F-NaF Positron-emission tomography (PET)-CT revealed increased uptake associated with the skull base and gnathic bones in all patients. In conclusion, this first detailed systematic evaluation of the craniofacial phenotype of patients with JMC demonstrates a distinct and pronounced phenotype that predominantly affects the NCC-derived cranial bones indicating a critical role of PTH1R signaling in their development. These affects can result in significant disease-related morbidity, include hearing loss, nerve compression, craniosynostosis, dentoskeletal malocclusion, and airway compromise; all of which require close monitoring.

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来源期刊
JBMR Plus
JBMR Plus Medicine-Orthopedics and Sports Medicine
CiteScore
5.80
自引率
2.60%
发文量
103
审稿时长
8 weeks
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